FDA Inspection 948193 — Proficient Rx LP

Proficient Rx LP — FEI 3011557028

The FDA completed an inspection of Proficient Rx LP on Oct 22, 2015 in Thousand Oaks, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 5 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 22, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Thousand Oaks, CA (United States)

Citations

IDCFRDescription
127021 CFR 211.68(b)input/output verification
358521 CFR 211.110(a)Control procedures to monitor and validate performance
430321 CFR 211.67(b)Written procedures fail to include
439121 CFR 211.180(e)(2)Items to cover on annual reviews
457621 CFR 211.192No written record of investigation